| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333962-103334252 | Common:1; Rare:121 | ||||
| chr14:103334254-103334551 | Common:5; Rare:109 | ||||
| chr14:103335445-103335493 | Rare:12 | ||||
| chr14:103529026-103529243 | Common:1; Rare:66 | ||||
| chr14:103561928-103562038 | Common:3; Rare:44 | ||||
| chr14:103562227-103562381 | Rare:65 | ||||
| chr14:103562615-103563015 | Common:6; Rare:143; Clinvar (benign):2 | ||||
| chr14:103629124-103629440 | Common:3; Rare:129 | ||||
| chr14:103673035-103673395 | Common:1; Rare:71 | ||||
| chr14:103715466-103715853 | Common:1; Rare:126 | ||||
| chr14:103921469-103921586 | Common:2; Rare:41 | ||||
| chr14:104772395-104772670 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:104775182-104775413 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:104924571-104924894 | Common:2; Rare:72 | ||||
| chr14:105021044-105021391 | Common:1; Rare:122 |